Clinical Scientist – Oncology

This is a fully remote position, open to applicants in United States.

📋 Description

• Assist the CS Protocol Lead and study team in the clinical/scientific execution of clinical studies

• Provide support for adjudication activities

• Aid in medical monitoring tasks

• Prepare for the reconciliation of imaging data

• Create materials for meetings

• Oversee management of protocol deviations

• Support either a single study or multiple studies

• Lead studies with a limited scope, such as Survival Follow-up

• Collaborate with cross-functional teams

• Engage with internal and external stakeholders, including study sites and committees, to support clinical study goals

• Complete necessary training, timesheets, and expense reports

• Update CV as needed

• Adhere to Parexel processes, ICH-GCPs, and other applicable regulations

⛳️ Requirements

• Experience in oncology is mandatory

• Bachelor's, Master's, or PhD in Life Sciences with a minimum of 2 years of relevant professional experience

• If lacking a degree in Life Sciences, a Bachelor's degree with substantial experience in clinical development (>5 years) is required

• Proven oral and written communication abilities

• Proficient in MS Office Suite, including Word, Excel, and PowerPoint

• Advanced skills in Excel, including the use of pivot tables and VLOOKUPs

• Strong command of written and spoken English

• Willingness to travel as necessary for important company meetings

• Pharmaceutical experience is advantageous but not essential

• Preferred 2 years of experience in medical monitoring

• Familiarity with adjudication support, medical monitoring, imaging data reconciliation, meeting materials preparation, and protocol deviation management

• Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs, and other applicable standards

🏝️ Benefits

• Equal opportunity employment

• Home-based/remote work arrangement